Canonical Allele Identifier: CA2787930264

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493322_49493329del , CM000672.2:g.49493322_49493329del	GRCh38
NC_000010.10:g.50701368_50701375del , CM000672.1:g.50701368_50701375del	GRCh37
NC_000010.9:g.50371374_50371381del	NCBI36
NG_009442.1:g.50773_50780del , LRG_465:g.50773_50780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1686-77_1686-70del MANE Select	ENSP00000348089.5:n.1686-77_1686-70del
ENST00000681632.1:n.1764-77_1764-70del
ENST00000681659.1:c.1527-77_1527-70del	ENSP00000505631.1:n.1527-77_1527-70del
ENST00000355832.9:c.1686-77_1686-70del	ENSP00000348089.5:n.1686-77_1686-70del
ENST00000475116.1:n.275+7209_275+7216del
ENST00000623073.3:c.87-77_87-70del	ENSP00000485650.1:n.87-77_87-70del
ENST00000623115.3:c.-70+7209_-70+7216del	ENSP00000485321.1:n.-70+7209_-70+7216del
ENST00000623318.1:c.87-77_87-70del	ENSP00000485423.1:n.87-77_87-70del
NM_000124.3:c.1686-77_1686-70del	NP_000115.1:n.1686-77_1686-70del
NM_001346440.1:c.1686-77_1686-70del	NP_001333369.1:n.1686-77_1686-70del
NM_000124.4:c.1686-77_1686-70del MANE Select	NP_000115.1:n.1686-77_1686-70del
NM_001346440.2:c.1686-77_1686-70del	NP_001333369.1:n.1686-77_1686-70del